Barely Significant
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Combining Genetic Variants to Improve Risk Prediction for NAFLD and Its Progression to Cirrhosis: A Proof of Concept Study.

Can J Gastroenterol Hepatol · 2018 · PMC5872672 · PMID 29732362

Europe PMCDOI
1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

nearly significantp < 0.001actually significant
At least one difference in allele frequency between groups was significant, or nearly significant, for the PNPLA3, TM6SF2, and KLF6 variants ( p < 0.001, p < 0.05, and p = 0.06, resp.), and a risk score based on these SNPs was generated.

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